Scandium triflate catalyzed ester synthesis using primary amides

Benjamin N. Atkinson; Jonathan M J Williams

doi:10.1016/j.tetlet.2014.10.124

Scandium triflate catalyzed ester synthesis using primary amides

Benjamin N. Atkinson, Jonathan M J Williams

Research output: Contribution to journal › Article › peer-review

20 Citations (SciVal)

Abstract

A scandium triflate (ScOTf)₃ catalyzed methodology has been developed to synthesize esters from primary amides. Various primary and secondary aliphatic alcohols have been shown to react in n-heptane with a range of primary amides for 24 h.

Original language	English
Pages (from-to)	6935-6938
Number of pages	4
Journal	Tetrahedron Letters
Volume	55
Issue number	50
Early online date	28 Oct 2014
DOIs	https://doi.org/10.1016/j.tetlet.2014.10.124
Publication status	Published - 10 Dec 2014

Keywords

Alcohols
Alcoholysis
Amides
Esters
Scandium

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10.1016/j.tetlet.2014.10.124

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title = "Scandium triflate catalyzed ester synthesis using primary amides",

abstract = "A scandium triflate (ScOTf)3 catalyzed methodology has been developed to synthesize esters from primary amides. Various primary and secondary aliphatic alcohols have been shown to react in n-heptane with a range of primary amides for 24 h.",

keywords = "Alcohols, Alcoholysis, Amides, Esters, Scandium",

author = "Atkinson, {Benjamin N.} and Williams, {Jonathan M J}",

year = "2014",

month = dec,

day = "10",

doi = "10.1016/j.tetlet.2014.10.124",

language = "English",

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journal = "Tetrahedron Letters",

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T1 - Scandium triflate catalyzed ester synthesis using primary amides

AU - Atkinson, Benjamin N.

AU - Williams, Jonathan M J

PY - 2014/12/10

Y1 - 2014/12/10

N2 - A scandium triflate (ScOTf)3 catalyzed methodology has been developed to synthesize esters from primary amides. Various primary and secondary aliphatic alcohols have been shown to react in n-heptane with a range of primary amides for 24 h.

AB - A scandium triflate (ScOTf)3 catalyzed methodology has been developed to synthesize esters from primary amides. Various primary and secondary aliphatic alcohols have been shown to react in n-heptane with a range of primary amides for 24 h.

KW - Alcohols

KW - Alcoholysis

KW - Amides

KW - Esters

KW - Scandium

UR - http://www.scopus.com/inward/record.url?scp=84910618660&partnerID=8YFLogxK

UR - http://dx.doi.org/10.1016/j.tetlet.2014.10.124

U2 - 10.1016/j.tetlet.2014.10.124

DO - 10.1016/j.tetlet.2014.10.124

M3 - Article

AN - SCOPUS:84910618660

SN - 0040-4039

VL - 55

SP - 6935

EP - 6938

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 50

ER -

Scandium triflate catalyzed ester synthesis using primary amides

Abstract

Keywords

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